Ocular Motor Findings Aid in Differentiation of Spinocerebellar Ataxia Type 17 from Huntington’s Disease
Author:
Funder
Ministry of Health and Welfare
Ministry of Education, Science and Technology
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s12311-021-01356-2.pdf
Reference65 articles.
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3. Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? Ann Neurol. 1997;42(6):924–32.
4. Bürk K, Zühlke C, König IR, Ziegler A, Schwinger E, Globas C, et al. Spinocerebellar ataxia type 5 Clinical and molecular genetic features of a German kindred. Neurology. 2004;62(2):327–9.
5. Jen JC, Yue Q, Karrim J, Nelson SF, Baloh RW. Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia. J Neurol Neurosurg Psychiatry. 1998;65(4):565–8.
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